Activation of a latent respiratory motor pathway by stimulation of neurons in the medullary chemoreceptor area of the rat

被引:8
|
作者
Zhou, SY [1 ]
Castro-Moure, F
Goshgarian, HG
机构
[1] Univ Michigan, Dept Internal Med, Ann Arbor, MI 48109 USA
[2] Wayne State Univ, Sch Med, Dept Anat & Cell Biol, Detroit, MI 48201 USA
[3] Highland Hosp, Div Neurosurg, Oakland, CA 94602 USA
关键词
chemoreceptor stimulation; glutamate metabotropic receptor; spinal cord injury; crossed phrenic phenomenon; respiration; phrenic nerve; respiratory stress;
D O I
10.1006/exnr.2001.7740
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Previous studies have demonstrated that during respiratory stress (hypercapnia and hypoxia), a latent crossed respiratory, pathway can be activated to produce hemidiaphragm recovery following an ipsilateral C2 spinal cord hemisection. The present study investigates the effects of ventral medullary chemoreceptor area stimulation by microinjection of (1S,3R)-aminocyclopentanedicarboxylic acid (ACPD), a glutamate metabotropic receptor agonist, on activating the latent pathway following left C2 spinal cord hemisection in rats in which end-tidal CO2 was maintained at a constant level. Experiments were conducted on anesthetized, vagotomized, paralyzed, and artificially ventilated rats in which phrenic nerve activity was recorded bilaterally. Before drug injection, the phrenic nerve contralateral to hemisection showed vigorous respiratory-related activity, but the phrenic nerve ipsilateral to hemisection showed no discernible respiratory-related activity. ACPD (1-100 nl, I mM) was injected directly into the region of the retrotrapezoid nucleus (RTN), a known medullary chemoreceptor area. Microinjection of ACPD into the right RTN increased respiratory-related activity in the right phrenic nerve (contralateral to hemisection). ACPD (>5 nl, I mM) microinjection also significantly induced respiratory recovery in the phrenic nerve ipsilateral to hemisection in a dose-dependent manner. The present study indicates that respiratory recovery can be achieved by stimulation of respiratory circuitry without increasing CO2 levels. (C) 2001 Academic Press.
引用
收藏
页码:176 / 184
页数:9
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